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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Genetic pathways involved in human speech disorders
Joery den Hoed, Simon E. Fisher
Current Opinion in Genetics & Development (2020) Vol. 65, pp. 103-111
Open Access | Times Cited: 35

Showing 1-25 of 35 citing articles:

Developmental mechanisms underlying the evolution of human cortical circuits
Pierre Vanderhaeghen, Franck Polleux
Nature reviews. Neuroscience (2023) Vol. 24, Iss. 4, pp. 213-232
Open Access | Times Cited: 92
Uncovering the genetic architecture of broad antisocial behavior through a genome-wide association study meta-analysis
Jorim J. Tielbeek, Emil Uffelmann, Benjamin Williams, et al.
Molecular Psychiatry (2022) Vol. 27, Iss. 11, pp. 4453-4463
Open Access | Times Cited: 41
Shared genetic liability and causal effects between major depressive disorder and insomnia
Ancha Baranova, Hongbao Cao, Fuquan Zhang
Human Molecular Genetics (2021) Vol. 31, Iss. 8, pp. 1336-1345
Closed Access | Times Cited: 38
Dissecting the neurobiology of linguistic disorganisation and impoverishment in schizophrenia
Lena Palaniyappan
Seminars in Cell and Developmental Biology (2021) Vol. 129, pp. 47-60
Closed Access | Times Cited: 36
Developmental disorders caused by haploinsufficiency of transcriptional regulators: a perspective based on cell fate determination
Roman Zug
Biology Open (2022) Vol. 11, Iss. 1
Open Access | Times Cited: 23
Neuroscience-Driven Solutions for Speech Impairment
Anil Chandra G. V. S., Shantagoud Biradar, Ramya Raghavan
Advances in medical education, research, and ethics (AMERE) book series (2025), pp. 119-146
Closed Access
A Biopsychosocial Overview of Speech Disorders: Neuroanatomical, Genetic, and Environmental Insights
Diya Jaishankar, Tanvi Raghuram, Bhuvanesh Kumar Raju, et al.
Biomedicines (2025) Vol. 13, Iss. 1, pp. 239-239
Open Access
Deciphering the genetic basis of developmental language disorder in children without intellectual disability, autism or apraxia of speech
Clothilde Ormières, Marion Lesieur‐Sebellin, Karine Siquier-Pernet, et al.
Molecular Autism (2025) Vol. 16, Iss. 1
Open Access
Sequence variants affecting voice pitch in humans
Rósa S. Gísladóttir, Agnar Helgason, Bjarni V. Halldórsson, et al.
Science Advances (2023) Vol. 9, Iss. 23
Open Access | Times Cited: 8
Heterozygous variants that disturb the transcriptional repressor activity of FOXP4 cause a developmental disorder with speech/language delays and multiple congenital abnormalities
Lot Snijders Blok, Arianna Vino, Joery den Hoed, et al.
Genetics in Medicine (2020) Vol. 23, Iss. 3, pp. 534-542
Open Access | Times Cited: 22
Dissecting the cross-trait effects of the FOXP2 GWAS hit on clinical and brain phenotypes in adults with ADHD
Gabriela Pessin Meyer, Bruna Santos da Silva, Cibele Edom Bandeira, et al.
European Archives of Psychiatry and Clinical Neuroscience (2022) Vol. 273, Iss. 1, pp. 15-24
Open Access | Times Cited: 14
What risk factors for Developmental Language Disorder can tell us about the neurobiological mechanisms of language development
Tessel Boerma, Sita M. ter Haar, Rachida Ganga, et al.
Neuroscience & Biobehavioral Reviews (2023) Vol. 154, pp. 105398-105398
Open Access | Times Cited: 5
The clinical and genetic spectrum of paediatric speech and language disorders
Jan Magielski, Sarah M. Ruggiero, Julie Xian, et al.
Brain (2024) Vol. 148, Iss. 2, pp. 663-674
Closed Access | Times Cited: 1
SETBP1variants outside the degron disrupt DNA-binding and transcription independent of protein abundance to cause a heterogeneous neurodevelopmental disorder
Maggie M. K. Wong, Rosalie A. Kampen, Ruth Braden, et al.
medRxiv (Cold Spring Harbor Laboratory) (2022)
Open Access | Times Cited: 7
The clinical and genetic spectrum of paediatric speech and language disorders in 52,143 individuals
Jan Magielski, Sarah M. Ruggiero, Julie Xian, et al.
medRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access | Times Cited: 1
Diagnostic Uncertainty in Childhood Motor Speech Disorders: A Review of Recent Tools and Approaches
Patricia McCabe, Johanna Korkalainen, Donna Thomas
Current Developmental Disorders Reports (2024) Vol. 11, Iss. 3, pp. 105-112
Open Access | Times Cited: 1
The phenotype of homozygous EMC10 variant: A new syndrome with intellectual disability and language impairment
Eliana Haddad-Eid, Noa Gur, Sharbel Eid, et al.
European Journal of Paediatric Neurology (2022) Vol. 37, pp. 56-61
Closed Access | Times Cited: 6
An Investigation of Barriers and Enablers for Genetics in Speech-Language Pathology Explored Through a Case Study of Childhood Apraxia of Speech
Mariana L. Lauretta, Anna Jarmolowicz, David J. Amor, et al.
Journal of Speech Language and Hearing Research (2023) Vol. 67, Iss. 9S, pp. 3437-3451
Closed Access | Times Cited: 3
Differences in Cortical Surface Area in Developmental Language Disorder
Nilgoun Bahar, Gabriel J. Cler, Saloni Krishnan, et al.
Neurobiology of Language (2023) Vol. 5, Iss. 2, pp. 288-314
Open Access | Times Cited: 3
Identification of FoxP circuits involved in locomotion and object fixation in Drosophila
Ottavia Palazzo, Mathias Raß, Björn Brembs
Open Biology (2020) Vol. 10, Iss. 12
Open Access | Times Cited: 8
Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family
Amaia Carrión-Castillo, Sara B. Estruch, Ben Maassen, et al.
Human Genetics (2021) Vol. 140, Iss. 8, pp. 1183-1200
Open Access | Times Cited: 7
Reply to: “Historical pursuits of the language pathway hypothesis of schizophrenia”
Lena Palaniyappan, Jingnan Du, Jie Zhang, et al.
Schizophrenia (2021) Vol. 7, Iss. 1
Open Access | Times Cited: 4
Genetic variability of FOXP2 and its targets CNTNAP2 and PRNP in frontotemporal dementia: A pilot study in a southern Italian population
Paolina Crocco, Francesco De Rango, Francesco Bruno, et al.
Heliyon (2024) Vol. 10, Iss. 11, pp. e31624-e31624
Open Access
Neurodevelopmental Disorders: Speech and Language Disorders
Michelle Palumbo, Maria Mody, William M. Klykylo, et al.
Springer eBooks (2024), pp. 1533-1559
Closed Access
Using FoxP2 to Distinguish Direct and Indirect Basal Ganglia Pathways for Vocal Learning in Songbirds
Aditi Jagannathan, Mira Nigudkar, Sarah W. Bottjer
bioRxiv (Cold Spring Harbor Laboratory) (2024)
Open Access
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